Anesthetics Flashcards

1
Q

Goal of general anesthesia

A

amnesia
analgesia
immobilization

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2
Q

Inhaled anesthetic properties

A

cross BBB

Lipid solubility - higher = more potent

blood solubility - lower = more rapid onset of action
-doens’t get “stuck in the blood”

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3
Q

Minimum alveolar concentration (MAC)

A

concentration of inhaled anesthetic needed to prevent movement in 50% of patients after painful stimulus

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4
Q

Inhaled anesthetic drugs

A

Nitrous oxide

  • low blood solubility (rapid induction), low lipid solubility (low potency)
  • block NMDA receptors
  • rapid onset/rapid recovery

Halothane

  • high blood solubility (long induction)
  • hepatotoxicity
  • long to start, long to recover

Sevoflurane, desflurane

  • low blood solubility, high lipid solubility
  • potent, most used

Isoflurane
-moderate blood and lipid solubility

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5
Q

Propofol

A

IV anesthetic

increases GABA
Rapid onset, rapid recovery (20-40min)
high triglyceride count - risk acute pancreatitis with prolonged use

“milk of amnesia”
maintenance in IV drip

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6
Q

Ketamine

A

IV anesthetic

dissociative anesthetic
hallucinations in high doses in adults
increases cerebral blood flow

use: analgesia, conscious sedation, induction

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7
Q

Barbiturates

A

IV anesthetics

Phenobarbital - increases liver enzyme synthesis (used in Crigler Najjar type II)
Pentobarbital
secobarbital
Thiopental (important in brain surgery)

increase duration of Cl- channel opening on GABA receptors

SE:
sedation, CNS depression, sluggish, ataxic gait, double vision

Overdose: tx sx, no antidote

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8
Q

Benzodiazepines

A

IV anesthetics

Diazepam
lorazepam
alprazolam
Midazolam - MC used for conscious sedation

Others:
Temazepam - insomnia - long acting
Chlordiazepoxide - etOH withdrawal

Increase frequency of Cl- channel opening on GABA receptors

Reverse w/ flumazenil (can trigger withdrawal seizure)

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9
Q

mnemonic for barbiturate and benzodiazepine MOA

A

“Ben likes it more frequently, Barb likes it to last longer”

effects on Cl- channel on GABA receptors

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10
Q

Opioids used as IVE anesthetics

A

morphine
fentanyl (doesn’t induce histamine release, not as itchy as with morphine)
remifentanil
sufentanil

Analgesia

mu, delta, kappa receptors

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11
Q

Butorphanol

A

partial opioid

causes respiratory depression

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12
Q

Dextromethorphan

A

weak opioid used for cough suppression

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13
Q

Tramadol

A

less addictive opioid used for analgesia

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14
Q

Loperamide, diphenoxylate

A

treatment of diarrhea

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15
Q

Naloxone, naltrexone

A

opioid receptor antagonists

reverse opioid overdose

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16
Q

Endogenous agonists of mu, delta, kappa receptors

A

Mu - beta-endorphin
Delta - enkephalin
Kappa - dynorphin

17
Q

Non-depolarizing NM blocking agents

A
tubocurarine
atracurium
mivacurium
vecuronium
rocuronium
pancuronium

Competitive inhibitors of postsynaptic nicotinic acetylcholine receptors at NMJ

can reverse w/ acetylcholinesterase inhibitor - neostigmine

18
Q

Depolarizing NM blocking agent

A

succinylcholine

causes muscle fasciculations

Phase 1: rapid onset and recovery, cannot be reversed - 10 min

Phase 2: larger dose, longer recovery - can be reversed w/ AChEI - lasts 20-30 minutes up to hours

Succinylcholine + inhaled anesthetic in patient with RYR1 gene mutation –> malignant hyperthermia
Tx: cool patient, sedate, dantrolene (block release of Ca2+ from SR)

19
Q

Local anesthetics

A

Lidocaine, procain, cocaine
block Na+ channels

Don’t work well in acidic tissues - infected tissues

give w/ local vasoconstrictor (epi)

  • except in terminal organs (eg fingers - no collateral circulation = ischemia)
  • don’t need as much anesthetic, reduces bleeding
20
Q

Order of blockade for local anesthetics

A

small myelinated
small unmyelinated
large myelinated